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Ags x 10 kn

Manufactured by Shimadzu
Sourced in Japan

The AGS-X 10 kN is a universal testing machine designed for a wide range of material and structural testing applications. It features a maximum load capacity of 10 kN and can perform tensile, compression, and flexural tests on a variety of materials. The system includes a high-precision load cell, an advanced control unit, and various grips and fixtures for secure specimen holding.

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13 protocols using ags x 10 kn

1

Mechanical Characterization of Materials

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The static tensile test was carried out according to (PN-EN ISO 527—type 1:2012) [29 ] on an MTS Criterion Model 43 universal testing machine (MTS System Corp., Eden Prairie, MN, USA) with an MTS axial extensometer. The measuring base was set to 100 mm, and the test speed was equal to 5 mm/min. The three-point flexural test (PN-EN ISO 178:2011) [30 ] was carried out using a Shimadzu AGS-X 10 kN (Kyoto, Japan) testing machine with TRAPEZIUM-X software, https://www.shimadzu.com/an/products/materials-testing/uni-ttm-software/trapezium-x/index.html. The distance between supports was set to 64 mm; test speed was 10 mm/min. The Charpy impact test was performed using a Zwick/Roell HIT5.5P hammer (Ulm, Germany) according to PN-EN ISO 179-1:2010 [31 ]. Measurements were examined on unnotched specimens.
Mechanical hysteresis loops were obtained by dynamic testing on a Shimadzu AGS-X 10 kN (Kyoto, Japan) testing machine with TRAPEZIUM-X software for dissipation energy analysis. The samples were subjected to cyclic loading and unloading at 10 mm/min speed. The applied force corresponded to 60% of the maximum force needed to break the sample, determined during the tensile test.
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2

Tensile Properties of Recycled Polypropylene

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For the tensile testing, ISO 527-2 [35 ] type 5 A specimens were obtained by injection molding with the mini injection machine HAAKE MiniJet II (Thermo Fisher Scientific, Waltham, MA, USA). The injection molding processing conditions of the virgin and recycled PP specimens are shown in Table 2.
The tensile tests were conducted on the machine Shimadzu AGS-X-10kN (Shimadzu Scientific Instruments (SSI), Columbia, MD, USA) following the standard ISO 527-1 [36 ]. These tests were executed at ambient temperature in two steps. First, the specimens were pulled with a tensile rate of 1 mm/min to obtain values for calculating the Young modulus. In the second stage, a tensile rate of 50 mm/min was applied and maintained until the specimens ruptured. The data from this second test was used to determine the yield stress (σy) and strain (εy), and tensile strength (σu) and strain at break (εb). It should be noted that the latter is especially relevant for the polymer degradation assessment because of this property’s extraordinary sensitivity to any structural change [37 (link)]. For each PP batch, five specimens were tested.
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3

Tip Compression Strength Evaluation

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The design was evaluated by recreating the bench test setup of Barkholt et al. [16 (link)]. With a GW in place, the tip was pressed against a plate with a hole slightly larger than the GW (0.36 mm). The tip was clamped into the universal testing machine Shimadzu AGS-X 10 kN (Shimadzu Corporation, Kyoto, Japan). The force required to compress the tip by 0.5 mm was recorded using a 200 N load cell with an accuracy of the measured value of ± 0.5% in the range of 0.4–200 N. Below 0.4 N, the accuracy of the measured value is reduced to ± 1%. While the GW can pass through the hole, the tip gets pressed against the plate. The damage of the tip was assessed by measuring the diameter before and after the test, respectively.
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4

Tensile Strength of Composite Samples

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The tensile strengths of the NW, DW, and TW samples were tested using a Shimadzu tensile testing machine (AGS-X 10KN, Kyoto City, Japan) with a gauge length of 40 mm, a tensile speed of 3 mm/min, and sample dimensions of 70 mm × 10 mm × 0.5 mm (L × W × H), and seven parallel samples were set up for each group of specimens and averaged with the results of the tests.
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5

Tensile Testing of Material Samples

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Tensile tests were performed according to ASTM D638-14 using a universal testing machine (AGS-X 10 kN, Shimadzu, Kyoto, Japan) with an axial extensometer (Model 3442, Epsilon Technology Corp, Jackson, WY, USA). The geometry of the samples was ASTM D638 Type V. Each formulation was tested at three crosshead speeds: 1, 10, and 100 mm min−1 with five samples per speed to determine sensitivity to high strain rates.
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6

Characterization of Ceramic Spheres

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The microstructures
of ceramic spheres were observed by a scanning electron microscope
(SEM, S8010, Hitachi). The crystalline phases of the samples were
characterized via X-ray diffraction (XRD, D8 Advance, Bruker). The
compressive strength of ceramic spheres was obtained using a universal
testing machine (AGS-X-10 kN, Shimadzu). The compressive strength
of the spheres is defined as the fracture load per their maximum cross-sectional
area, and the average strength was obtained by measuring 10 samples
for each at each data point,37 (link) which has
been added in the revised manuscript. Fourier transform infrared (FTIR)
spectroscopy was performed on a Nicolet iN10 FT-IR microscope (Thermo
Nicolet Corp.). The morphologies and EDX analysis of the specimens
were obtained on a transmission electron microscopy (TEM, JEOL-2100Plus).
N2 adsorption/desorption isotherms of samples were determined
via a surface area analyzer (TriStar I13020, Micromerities). Pore
size distribution and the specific surface area were obtained by the
BJH method and BET method, respectively.
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7

Compression Testing of Specimens

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The specimens for testing were prepared and the compression tests were made according to ASTM F451-16 standard with the Shimadzu AGS-X 10KN (Shimadzu Corp., Kyoto, Japan) machine at compression velocity 20 mm/min. The load and displacement were continuously recorded. The failure loading criterion was defined according to the above standard at 2% offset upper yield point or the fracture.
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8

Mechanical Properties Assessment of Biomaterials

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The assessment of the mechanical properties after different periods of immersion (15, 30, and 45 days) in DMEM/F-12 supplemented with 10% FBS was performed using the tensile assay according to ASTM E8 [27 (link)]. Immersion conditions and samples surface to medium volume ratio were the same as those described in Section 2.5, but specimens were allocated in individual 3D-printed ABS holders specifically designed to allow homogeneous exposure of bone-shaped specimens to the immersion medium. Three samples for each period were considered for the tensile tests, carried out in a universal testing machine (Shimadzu AGS-X 10 kN, Jiangsu, China) at 0.1 mm/min testing speed (strain rate 1.6 × 10−4 s−1).
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9

Mechanical Characterization of Polypropylene

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The static tensile test and initial mechanical hysteresis loops were conducted using Shimadzu AGS-X 10 kN (Kyoto, Japan) testing machine. Tensile test was carried out in accordance with PN-EN ISO 527 standard. The crosshead speed was 5 mm/min. The test used cyclically loaded deformation to a maximum of 900 N (960 N is max. force for neat PP) to 400 N minimum and changes in maximum displacement were observed. The speed of load and unload specimens was 100 mm/min, which is translated into a low frequency of cycles and allows visualization of viscosity phenomena.
The three-point bending test was performed on the MTS Criterion 43 (Minnesota, United States) universal testing machine with the MTS software TestSuites 1.0 in accordance with PN-EN ISO 178 standard. The crosshead speed was10 mm/min.
The impact test was carried out using the Charpy method on a Zwick/Roell MTS-SP testing machine (Ulm, Germany), in accordance with the PN-EN ISO 179 standard. The samples were unnotched. The impact energy was 2 and 5J.
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10

Mechanical and Luminescence Analysis of Specimens

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The mechanical strengths of the specimens were examined by the pressure testing machine TYE-300 purchased from Wuxi Jianyi Instrument Machinery Co., Ltd. The test process followed the P.R.C standard ‘‘GB/T 17,671–199929 . The photoluminescence excitation (PLE), photoluminescence (PL) and persistent luminescence (PSL) spectra were detected by fluorescence spectrometer (FP-8600, JASCO Co., Japan), equipped with a 150 W Xe lamp. The mechanoluminescence (ML) intensity of specimen under extra stress was measured with a lab-made system comprising a universal testing machine (AGS-X10kN, Shimadzu Corp., Japan) and a photomultiplier tube (C13796, Hamamatsu Photonics, Japan). The ML spectrum of specimen was examined by fiber spectrometer (QE Pro, Ocean Optics) collocated with the universal testing machine.
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